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HRID 967312作成日:2026年10月25日

Glutaric anhydride → 5-(4-[(4aS,8aR)-4-(3,4-Diethoxy-phenyl)-1-oxo-4a,5,8,8a-tetrahydro-1H-phthalazin-2-yl]-piperidin-1-yl)-5-oxo-pentanoic Acid

https://huagongshe.com/reaction/967312

反応式

関与物質

役割名称HCID仕込み量
反応物Glutaric anhydrideHCID 7940—
反応物(4aS,8aR)-4-(3,4-Diethoxyphenyl)-2-[1-(toluene-4-sulfonyl)-piperidin-4-yl]-4a,5,8,8a-tetrahydro-2H-phthalazin-1-oneHCID 10175016—
生成物5-(4-[(4aS,8aR)-4-(3,4-Diethoxy-phenyl)-1-oxo-4a,5,8,8a-tetrahydro-1H-phthalazin-2-yl]-piperidin-1-yl)-5-oxo-pentanoic AcidHCID 10196063—

反応手順

Prepared from glutaric anhydride and starting compound A2 as described for compound 1. After evaporating the pyridine, the residue is partitioned between ethyl acetate and 1N hydrochloric acid. The ethyl acetate solution is dried over magnesium sulfate and evaporated. Crystallisation from diethyl ether. M. p. 133-135° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06953853B2
出典データセットuspto-grants-2005_10
ORD IDord-aa14bee00c2d41e4aef49e9d938faaad
出典メモuspto-grants-2005_10